A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511431



Internal ID20884758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51941811..51946991hg38UCSC Ensembl
chr15:52234008..52239188hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg385181
hg195181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024040
Samples
Known GenesLEO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511431
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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